Assistant Manager - QAU

Salary from 7.00 LPA To 10.00 LPA Negotiable based on current salary and experience.

The job description is as below:

Perform and oversee audits (facility-based, process-based, and study-based) as per OECD GLP guidelines.

Review and verify raw data, reports, and study plans for compliance with applicable GLP standards.

Ensure that standard operating procedures (SOPs) are current and being followed across departments.

Monitor the conduct of pharmacology, toxicology and analytical studies to ensure regulatory compliance.

Participate in regulatory inspections and ensure laboratory preparedness.

Maintain audit schedules, documentation, and deviation tracking systems.

Provide training and guidance on GLP compliance and QAU processes to laboratory personnel.

Support in drafting Quality Assurance Statements and internal audit reports.

Skills and Competencies:

Strong understanding of OECD GLP principles and regulatory requirements.

Hands-on experience with auditing techniques and documentation review.

Good communication and interpersonal skills.

High attention to detail and analytical thinking.

Ability to work independently and as part of a cross-functional team.

Preferred Experience:

Prior experience in QAU department in GLP environment.

Exposure to regulatory audits (e.g., OECD, NABL, FDA, AAALAC, etc.).

Experience with digital data systems and QA documentation tools.

Salary from 7.00 LPA To 10.00 LPA Negotiable based on current salary and experience.

For further details call Megha on or you can mail your candidature on